E-LIB Suche - Ergebnisse für: Mosbah, Helena

1

Partial lipodystrophy: Clinical presentation and treatment:

Mosbah, Héléna ; Vatier, Camille ; Vigouroux, Corinne
Annales d'Endocrinologie. 85 (2024) 3 - p. 197-200 , 2024

Link: https://doi.org/10.1016/..

2

Diagnostic and referral pathways in patients with rare lipo..:

Donadille, Bruno ; Janmaat, Sonja ; Mosbah, Héléna...
Orphanet Journal of Rare Diseases. 19 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

3

Autoimmune Addison's disease in the preclinical period mimi..:

Cadart, Olivier ; Biancheri Mounicq, Ingrid ; Lurton, Dominique..
Annales d'Endocrinologie. 85 (2024) 1 - p. 82-84 , 2024

Link: https://doi.org/10.1016/..

4

Leptin replacement therapy in the management of lipodystrop..:

Vigouroux, Corinne ; Mosbah, Héléna ; Vatier, Camille
Annales d'Endocrinologie. 85 (2024) 3 - p. 201-204 , 2024

Link: https://doi.org/10.1016/..

5

Primary disease of adipose tissue: When to think about and ..:

Vatier, Camille ; Vigouroux, Corinne ; Mosbah, Héléna
Annales d'Endocrinologie. 85 (2024) 3 - p. 190-194 , 2024

Link: https://doi.org/10.1016/..

6

A Family with a Single LMNA Mutation Illustrates Diversity ..:

Giguet-Valard, Anna-Gaëlle ; Monfort, Astrid ; Lucron, Hugues...
Cardiogenetics. 13 (2023) 4 - p. 135-144 , 2023

Link: https://doi.org/10.3390/..

7

Patients' perspective on the medical pathway from first sym..:

Mosbah, Héléna ; Vatier, Camille ; Andriss, Béatrice...
European Journal of Endocrinology. 190 (2023) 1 - p. 23-33 , 2023

Link: https://doi.org/10.1093/..

8

Proceedings of the annual meeting of the European Consortiu..:

Mosbah, Héléna ; Akinci, Baris ; Araújo-Vilar, David...
Annales d'Endocrinologie. 83 (2022) 6 - p. 461-468 , 2022

Link: https://doi.org/10.1016/..

9

Molecular and Cellular Bases of Lipodystrophy Syndromes:

Zammouri, Jamila ; Vatier, Camille ; Capel, Emilie...
Frontiers in Endocrinology. 12 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

10

Therapeutic indications and metabolic effects of metrelepti..:

Mosbah, Héléna ; Vantyghem, Marie‐Christine ; Nobécourt, Estelle...
Diabetes, Obesity and Metabolism. 24 (2022) 8 - p. 1565-1577 , 2022

Link: https://doi.org/10.1111/..

11

Rare genetic causes of obesity: Diagnosis and management in..:

Dubern, Béatrice ; Mosbah, Héléna ; Pigeyre, Marie..
Annales d'Endocrinologie. 83 (2022) 1 - p. 63-72 , 2022

Link: https://doi.org/10.1016/..

12

Bone Health in Adults With Prader–Willi Syndrome: Clinical ..:

van Abswoude, Denise H ; Pellikaan, Karlijn ; Rosenberg, Anna G W...
The Journal of Clinical Endocrinology & Metabolism. 108 (2022) 1 - p. 59-84 , 2022

Link: https://doi.org/10.1210/..

13

Hyponatremia in Children and Adults with Prader–Willi Syndr..:

Coupaye, Muriel ; Pellikaan, Karlijn ; Goldstone, Anthony P....
Journal of Clinical Medicine. 10 (2021) 16 - p. 3555 , 2021

Link: https://doi.org/10.3390/..

14

Effects of the COVID-19 pandemic and lockdown on the mental..:

Mosbah, Helena ; Coupaye, Muriel ; Jacques, Flavien...
Orphanet Journal of Rare Diseases. 16 (2021) 1 - p. , 2021

Link: https://doi.org/10.1186/..

15

Cardiovascular complications of lipodystrophic syndromes – ..:

Mosbah, Helena ; Vatier, Camille ; Boccara, Franck...
Annales d'Endocrinologie. 82 (2021) 3-4 - p. 146-148 , 2021

Link: https://doi.org/10.1016/..